A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622660



Internal ID6662829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:25185142..25201869hg38UCSC Ensembl
Innerchr10:25185174..25201837hg38UCSC Ensembl
Outerchr10:25185110..25201901hg38UCSC Ensembl
chr10:25474071..25490798hg19UCSC Ensembl
Innerchr10:25474103..25490766hg19UCSC Ensembl
Outerchr10:25474039..25490830hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3816728
hg1916728
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13721450
SamplesNA19375
Known GenesGPR158
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622660
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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